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铁(II)催化的亚砜与α-酰氧基酰胺的氮烯转移反应。

Iron(II)-Catalyzed Nitrene Transfer Reaction of Sulfoxides with -Acyloxyamides.

作者信息

Qi Tianxing, Fang Ning, Huang Weimin, Chen Jianhui, Luo Yanshu, Xia Yuanzhi

机构信息

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China.

出版信息

Org Lett. 2022 Aug 12;24(31):5674-5678. doi: 10.1021/acs.orglett.2c01990. Epub 2022 Aug 2.

Abstract

An iron(II)-catalyzed nitrene transfer reaction of sulfoxides with -acyloxyamides has been developed, leading to the efficient construction of acyl sulfoximines with high functional-group compatibility. The current catalytic transformation was carried out under an air atmosphere at ambient temperature and could be scaled up to gram scale with a catalyst loading of 1 mol %. Application of the methodology was demonstrated by facile C-H acetoxylation and olefination using the acyl sulfoximine as the directing group.

摘要

已开发出一种铁(II)催化的亚砜与酰氧基酰胺的氮烯转移反应,可高效构建具有高官能团兼容性的酰基亚砜亚胺。当前的催化转化在空气气氛下于室温进行,且催化剂负载量为1 mol%时可放大至克级规模。使用酰基亚砜亚胺作为导向基团,通过简便的C-H乙酰氧基化和烯烃化反应证明了该方法的实用性。

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